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The anti-craving compound acamprosate acts as a weak NMDA-receptor antagonist, but modulates NMDA-receptor subunit expression similar to memantine and MK-801.

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Rammes,  G.
Max Planck Institute of Psychiatry, Max Planck Society;

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Zieglgänsberger,  W.
Max Planck Institute of Psychiatry, Max Planck Society;

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Rammes, G., Mahal, B., Putzke, J., Parsons, C., Spielmanns, P., Pestel, E., et al. (2001). The anti-craving compound acamprosate acts as a weak NMDA-receptor antagonist, but modulates NMDA-receptor subunit expression similar to memantine and MK-801. Neuropharmacology, 40, 749-760.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-A426-1
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